Network-based inference framework for identifying cancer genes from gene expression data.

Great efforts have been devoted to alleviate uncertainty of detected cancer genes as accurate identification of oncogenes is of tremendous significance and helps unravel the biological behavior of tumors. In this paper, we present a differential network-based framework to detect biologically meaning...

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Publicado en:BioMed Research International Vol. 2013; pp. 401649 - 401650
Autores principales: Yang, Bo, Zhang, Junying, Yin, Yaling, Zhang, Yuanyuan
Formato: research Journal Article
Publicado: Wiley-Blackwell 2013
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 2013
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        atl: Network-based inference framework for identifying cancer genes from gene expression data.
      aug:
        au:
          Yang, Bo
          Zhang, Junying
          Yin, Yaling
          Zhang, Yuanyuan
        affil: School of Computer Science and Technology, Xidian University, Xi'an 710071, China.
      sug:
        subj:
          Resource Databases
          Genes
          Molecular Structure
          Oncogenes
          Neoplasms
          Algorithms
          Breast Neoplasms
          Computer Simulation
          Female
          Genetic Research
          Human
          Sequence Analysis
          ROC Curve
          Weights and Measures
          Signal Transduction
          Tumor Markers, Biological
          Female
      ab: Great efforts have been devoted to alleviate uncertainty of detected cancer genes as accurate identification of oncogenes is of tremendous significance and helps unravel the biological behavior of tumors. In this paper, we present a differential network-based framework to detect biologically meaningful cancer-related genes. Firstly, a gene regulatory network construction algorithm is proposed, in which a boosting regression based on likelihood score and informative prior is employed for improving accuracy of identification. Secondly, with the algorithm, two gene regulatory networks are constructed from case and control samples independently. Thirdly, by subtracting the two networks, a differential-network model is obtained and then used to rank differentially expressed hub genes for identification of cancer biomarkers. Compared with two existing gene-based methods (t-test and lasso), the method has a significant improvement in accuracy both on synthetic datasets and two real breast cancer datasets. Furthermore, identified six genes (TSPYL5, CD55, CCNE2, DCK, BBC3, and MUC1) susceptible to breast cancer were verified through the literature mining, GO analysis, and pathway functional enrichment analysis. Among these oncogenes, TSPYL5 and CCNE2 have been already known as prognostic biomarkers in breast cancer, CD55 has been suspected of playing an important role in breast cancer prognosis from literature evidence, and other three genes are newly discovered breast cancer biomarkers. More generally, the differential-network schema can be extended to other complex diseases for detection of disease associated-genes.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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